Shihui Yu

1.2k total citations
34 papers, 627 citations indexed

About

Shihui Yu is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shihui Yu has authored 34 papers receiving a total of 627 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shihui Yu's work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (7 papers) and Prenatal Screening and Diagnostics (5 papers). Shihui Yu is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (7 papers) and Prenatal Screening and Diagnostics (5 papers). Shihui Yu collaborates with scholars based in China, United States and Nigeria. Shihui Yu's co-authors include Douglas C. Bittel, W. Graf, Stephanie D. Fiedler, Nataliya Kibiryeva, David L. Zwick, Julie M. Joyce, Hongyu Liu, Arivudainambi Ramalingam, Linda D. Cooley and Ahmed Abdelmoity and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Shihui Yu

30 papers receiving 604 citations

Peers

Shihui Yu

GENET

PRM

PPCH

Maria Descartes United States

Gülen Eda Ütine Türkiye

Karen J. Harrison Canada

Chantal Missirian France

Josephine Wincent Sweden

Meena Balasubramanian United Kingdom

Elisa Tassano Italy

Chin‐To Fong United States

Olaf Rittinger Austria

Anita Wischmeijer Italy

Maria Descartes United States

Shihui Yu

431 ×1.2

GENET

399 ×1.2

62 ×0.6

PRM

94 ×1.0

PPCH

60 ×0.9

Citations per year, relative to Shihui Yu Shihui Yu (= 1×) peers Maria Descartes

Countries citing papers authored by Shihui Yu

Since Specialization

Citations

This map shows the geographic impact of Shihui Yu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Shihui Yu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shihui Yu more than expected).

Fields of papers citing papers by Shihui Yu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shihui Yu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Shihui Yu. The network helps show where Shihui Yu may publish in the future.

Co-authorship network of co-authors of Shihui Yu

This figure shows the co-authorship network connecting the top 25 collaborators of Shihui Yu. A scholar is included among the top collaborators of Shihui Yu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Shihui Yu. Shihui Yu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Zhu, Yan, Shihui Yu, Dan Yang, et al.. (2025). Integrated Multi-Omics Analysis Unveils Distinct Molecular Subtypes and a Robust Immune–Metabolic Prognostic Model in Clear Cell Renal Cell Carcinoma. International Journal of Molecular Sciences. 26(7). 3125–3125. 1 indexed citations

Song, Yuelin, Xia Yang, Yuhuan Meng, et al.. (2025). Genetic features and pharmacological rescue of novel Kv7.2 variants in patients with epilepsy. Journal of Medical Genetics. 62(4). 231–241.

Chen, Tao, et al.. (2023). MYD88-Mutated Chronic Lymphocytic Leukaemia/Small Lymphocytic Lymphoma as a Distinctive Molecular Subgroup Is Associated with Atypical Immunophenotypes in Chinese Patients. Journal of Clinical Medicine. 12(7). 2667–2667. 2 indexed citations

Hu, Dongsheng, Yaping Liu, Ling Yang, et al.. (2023). Sporadic lymphangioleiomyomatosis in a man with somatic mosaicism of TSC2 mutations, a case report. QJM. 117(1). 75–76.

Chen, Yuxin, Yuhuan Meng, Tao Chen, et al.. (2023). Machine learning models-based on integration of next-generation sequencing testing and tumor cell sizes improve subtype classification of mature B-cell neoplasms. Frontiers in Oncology. 13. 1160383–1160383.

Mao, Linlin, Weiwei Zhao, Xiaoxia Li, et al.. (2021). Mutation Spectrum of EGFR From 21,324 Chinese Patients With Non-Small Cell Lung Cancer (NSCLC) Successfully Tested by Multiple Methods in a CAP-Accredited Laboratory. Pathology & Oncology Research. 27. 602726–602726. 17 indexed citations

Wang, Ying, Tienan Wang, Jianchao Li, et al.. (2021). Functional Verification of Novel ELMO1 Variants by Live Imaging in Zebrafish. Frontiers in Cell and Developmental Biology. 9. 723804–723804. 3 indexed citations

Liu, Jie, Weiwei Zhao, Xiaohua Ou, et al.. (2019). Mutation spectrums of TSC1 and TSC2 in Chinese women with lymphangioleiomyomatosis (LAM). PLoS ONE. 14(12). e0226400–e0226400. 2 indexed citations

Zhao, Weiwei, Menghua Wu, Shuai Jiang, et al.. (2015). Robertsonian Translocations: An Overview of 872 Robertsonian Translocations Identified in a Diagnostic Laboratory in China. PLoS ONE. 10(5). e0122647–e0122647. 33 indexed citations

10.

Bittel, Douglas C., Nataliya Kibiryeva, Stephanie D. Fiedler, et al.. (2014). Ultra High-Resolution Gene Centric Genomic Structural Analysis of a Non-Syndromic Congenital Heart Defect, Tetralogy of Fallot. PLoS ONE. 9(1). e87472–e87472. 11 indexed citations

11.

Pichon, Jean‐Baptiste Le, Shihui Yu, Nataliya Kibiryeva, W. Graf, & Douglas C. Bittel. (2013). Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome. European Journal of Human Genetics. 21(10). 1093–1099. 16 indexed citations

12.

Abdelmoity, Ahmed, et al.. (2012). 15q11.2 Proximal Imbalances Associated With a Diverse Array of Neuropsychiatric Disorders and Mild Dysmorphic Features. Journal of Developmental & Behavioral Pediatrics. 33(7). 570–576. 30 indexed citations

13.

Yu, Shihui, W. Graf, & Robert J. Shprintzen. (2012). Genomic disorders on chromosome 22. Current Opinion in Pediatrics. 24(6). 665–671. 14 indexed citations

14.

Ramalingam, Arivudainambi, et al.. (2011). 16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders. Journal of Human Genetics. 56(7). 541–544. 97 indexed citations

15.

Abdelmoity, Ahmed, et al.. (2010). 1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay. European Journal of Medical Genetics. 54(2). 198–203. 26 indexed citations

16.

Yu, Shihui, et al.. (2010). Genomic profile of copy number variants on the short arm of human chromosome 8. European Journal of Human Genetics. 18(10). 1114–1120. 32 indexed citations

17.

Butler, Merlin G., Douglas C. Bittel, Nataliya Kibiryeva, Linda D. Cooley, & Shihui Yu. (2010). An interstitial 15q11‐q14 deletion: Expanded Prader‐Willi syndrome phenotype. American Journal of Medical Genetics Part A. 152A(2). 404–408. 15 indexed citations

18.

Yu, Shihui, Lei Shao, Howard W. Kilbride, & David L. Zwick. (2010). Haploinsufficiencies of FOXF1 and FOXC2 genes associated with lethal alveolar capillary dysplasia and congenital heart disease. American Journal of Medical Genetics Part A. 152A(5). 1257–1262. 47 indexed citations

19.

Yu, Shihui, et al.. (2009). Quantitative Real-Time Polymerase Chain Reaction for the Verification of Genomic Imbalances Detected by Microarray-Based Comparative Genomic Hybridization. Genetic Testing and Molecular Biomarkers. 13(6). 751–760. 25 indexed citations

20.

Yu, Shihui, et al.. (1993). Haptoglobin Types in Chinese Ethnic Groups. Human Heredity. 43(2). 131–133. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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